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Consequence of Elevated Fibroblast Growth Factor 23 Levels in Acute Kidney Injury, Renal Recovery and Overall Survival in Intensive Care Unit Patients After Major Surgery. (CROSBI ID 257644)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Sakan, Sanja ; Premužić, Vedran ; Bandić Pavlović, Danijela ; Bašić-Jukić, Nikolina Consequence of Elevated Fibroblast Growth Factor 23 Levels in Acute Kidney Injury, Renal Recovery and Overall Survival in Intensive Care Unit Patients After Major Surgery. // Therapeutic apheresis and dialysis, 22 (2018), 5; 544-551. doi: 10.1111/1744-9987.12703

Podaci o odgovornosti

Sakan, Sanja ; Premužić, Vedran ; Bandić Pavlović, Danijela ; Bašić-Jukić, Nikolina

engleski

Consequence of Elevated Fibroblast Growth Factor 23 Levels in Acute Kidney Injury, Renal Recovery and Overall Survival in Intensive Care Unit Patients After Major Surgery.

The main goal of our study was to investigate the role of increased fibroblast growth factor 23 (FGF23) levels on renal recovery and overall survival. We conducted a prospective case-control cohort study, which included 121 adult cases who developed AKI after major surgical procedures. The subjects were followed-up until the last enrolled patient survived 180 days or until the time of death. Higher FGF23 levels positively correlated with serum creatinine levels (P < 0.05). Significantly higher number of patients without diuresis and with FGF23 ≤ 709 RU/mL survived when compared to patients without diuresis and with FGF23 ≥ 709 RU/mL (P < 0.001). FGF23 levels >709 RU/mL were a good predictive tool for overall mortality in a 6-month period (P < 0.05). This is the first study to analyze the impact of FGF23 values on short-term renal recovery and survival of patients with AKI after major surgery. The FGF23 increase related to AKI especially in more severe stages and in patients without diuresis is an independent risk factor for mortality.

acute kidney injury ; fibroblast growth factor 23 ; mortality ; prognosis

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Podaci o izdanju

22 (5)

2018.

544-551

objavljeno

1744-9979

1744-9987

10.1111/1744-9987.12703

Povezanost rada

nije evidentirano

Poveznice
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